Incidental Mutation 'IGL02214:A330008L17Rik'
ID284792
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol A330008L17Rik
Ensembl Gene ENSMUSG00000052479
Gene NameRIKEN cDNA A330008L17 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.189) question?
Stock #IGL02214
Quality Score
Status
Chromosome8
Chromosomal Location99416642-99733438 bp(+) (GRCm38)
Type of Mutationintron
DNA Base Change (assembly) T to A at 99421758 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000064349
SMART Domains Protein: ENSMUSP00000070165
Gene: ENSMUSG00000052479

DomainStartEndE-ValueType
transmembrane domain 54 76 N/A INTRINSIC
transmembrane domain 115 137 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153366
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161597
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9430097D07Rik T C 2: 32,574,724 probably benign Het
A930004D18Rik A G 2: 18,027,256 L17P unknown Het
Abca14 A T 7: 120,294,175 M1283L probably benign Het
Adarb1 A T 10: 77,322,301 V104E probably damaging Het
Ano1 T A 7: 144,655,708 N252Y possibly damaging Het
Atp6v0a1 A G 11: 101,039,840 S498G probably benign Het
Bdp1 A G 13: 100,041,535 V1942A probably benign Het
Carf T A 1: 60,148,081 D579E probably damaging Het
Cltc A T 11: 86,732,586 S200R probably benign Het
Cpeb1 T C 7: 81,372,057 S113G possibly damaging Het
Csgalnact1 C A 8: 68,401,492 G219V probably damaging Het
Ehd3 T A 17: 73,820,546 L158H probably damaging Het
Etfa C A 9: 55,464,811 G289W probably damaging Het
Fndc3c1 G A X: 106,425,829 T1029I probably benign Het
Gipr C A 7: 19,157,546 G402V possibly damaging Het
Gm5724 T A 6: 141,723,185 D507V possibly damaging Het
Hacd1 C T 2: 14,026,947 V242M probably damaging Het
Hecw1 A G 13: 14,300,393 L520P probably damaging Het
Ibtk A T 9: 85,714,179 probably benign Het
Igkv16-104 A C 6: 68,425,794 I24L probably benign Het
Kcnh8 A T 17: 52,877,911 Y407F possibly damaging Het
Mansc1 C T 6: 134,610,360 V285M probably benign Het
Mindy4 A G 6: 55,216,651 R110G possibly damaging Het
Morn1 C T 4: 155,092,319 H100Y probably damaging Het
Naip6 A T 13: 100,316,059 S165T probably damaging Het
Olfr1110 T G 2: 87,135,505 K272T probably damaging Het
Olfr538 A T 7: 140,574,557 R135* probably null Het
Prx G T 7: 27,518,912 R946M probably damaging Het
Ptchd1 A G X: 155,573,710 V833A possibly damaging Het
Rgl2 A G 17: 33,935,189 D481G probably benign Het
Serpinb3a A G 1: 107,048,488 probably null Het
Shtn1 T C 19: 58,999,886 probably benign Het
Sult1b1 C T 5: 87,535,090 probably benign Het
Tbl3 T C 17: 24,704,132 probably benign Het
Trappc9 C T 15: 73,012,882 W416* probably null Het
Ubr4 G A 4: 139,461,827 probably null Het
Ubr4 T C 4: 139,428,583 Y2240H possibly damaging Het
Vmn2r76 A C 7: 86,229,930 F387L probably benign Het
Vps8 G A 16: 21,517,285 C729Y probably damaging Het
Other mutations in A330008L17Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01067:A330008L17Rik APN 8 99421954 intron noncoding transcript
IGL03305:A330008L17Rik APN 8 99419830 unclassified probably benign
IGL03348:A330008L17Rik APN 8 99421692 intron noncoding transcript
LCD18:A330008L17Rik UTSW 8 99723425 intron noncoding transcript
R0173:A330008L17Rik UTSW 8 99421654 intron noncoding transcript
R1756:A330008L17Rik UTSW 8 99421882 intron noncoding transcript
R3829:A330008L17Rik UTSW 8 99421757 intron noncoding transcript
Posted On2015-04-16